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FDA 510(k)

NEXUS LIGATING CLIP

K-Number: K053255 · 2006-03-14

Decision Date2006-03-14
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEXUS LIGATING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Microsurgical Laboratories,Inc.Dba Wexler Surgical. It received FDA 510(k) clearance on 2006-03-14 under 510(k) number K053255. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXUS LIGATING CLIP?

NEXUS LIGATING CLIP is a medical device that received FDA 510(k) clearance on 2006-03-14. The listed applicant is Microsurgical Laboratories,Inc.Dba Wexler Surgical. The 510(k) number is K053255.

When did NEXUS LIGATING CLIP receive FDA 510(k) clearance?

NEXUS LIGATING CLIP received FDA 510(k) clearance on 2006-03-14, under 510(k) number K053255.

Who is the listed applicant for NEXUS LIGATING CLIP?

The FDA 510(k) record lists Microsurgical Laboratories,Inc.Dba Wexler Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEXUS LIGATING CLIP?

The FDA product code for NEXUS LIGATING CLIP is FZP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Microsurgical Laboratories,Inc.Dba Wexler Surgical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FZP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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